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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769683Generated: October 31, 2026

Thiophene → HCID 53754573, compound

https://huagongshe.com/reaction/1769683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 53854495HCID 53854495—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 53754573HCID 5375457339%

Reaction Steps

A mixture of N-(4-nitro-2,6-dichlorophenyl)-4-formyl-1-piperazineacetamide (1.79 g crude) was suspended in methanol (50 mL) containing 4% methanolic thiophene (0.5 mL) and 5% platinum on charcoal catalyst (900 mg). This was hydrogenated using a Parr apparatus for 30 minutes at 50° C. and 26 psi. After filtration and the removal of solvent in vacuo, the filtrate yielded 1.38 g of crude residue. This was subjected to flash chromatography on deactivated silica gel (from a slurry of 300 g of silica gel in methylene chloride containing 3.4 mL of conc. NH4OH). The product was eluted with CH2Cl2 :MeOH:NH4OH 98.8:1.0:0.2 yielding 590 mg of III an off-white solid. This was triturated in methylene chloride-ether to yield a white solid (520 mg, 39% yield).: m.p.>220° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382584
Source datasetuspto-grants-1995_01
ORD IDord-f8c900d661c44be09050d2c2b1cac2b7
Source noteuspto-grants-1995_01